TY - JOUR
T1 - Development of Novel Mouse Monoclonal Antibodies against Human CD19
AU - Yamada, Shinji
AU - Kaneko, Mika K.
AU - Sayama, Yusuke
AU - Asano, Teizo
AU - Sano, Masato
AU - Yanaka, Miyuki
AU - Nakamura, Takuro
AU - Okamoto, Saki
AU - Handa, Saori
AU - Komatsu, Yu
AU - Nakamura, Yoshimi
AU - Furusawa, Yoshikazu
AU - Takei, Junko
AU - Kato, Yukinari
N1 - Funding Information:
This research was supported, in part, by Japan Agency for Medical Research and Development (AMED), Grant Numbers: JP19am0401013 (Y.K.), JP19am0101078 (Y.K.), and JP19ae0101028 (Y.K.), and by Japan Society for the Promotion of Science (JSPS) KAKENHI, Grant Numbers: 17K07299 (M.K.K.) and 19K07705 (Y.K.).
Publisher Copyright:
© Copyright 2020, Mary Ann Liebert, Inc., publishers 2020.
PY - 2020/4
Y1 - 2020/4
N2 - CD19 is a type I transmembrane glycoprotein belonging to the immunoglobulin superfamily. It is expressed in normal and neoplastic B cells, and it modulates the threshold of B cell activation for amplifying B cell receptor signaling. Blinatumomab (a CD3-CD19-bispecific T cell-engaging antibody) and tisagenlecleucel (genetically modified T cells that express a CD19 chimeric antigen receptor [CART-19]) provide significant benefits for patients with CD19-positive relapsed or refractory B cell malignancies. In this study, we first employed the Cell-Based Immunization and Screening (CBIS) method to produce anti-CD19 monoclonal antibodies using CD19-overexpressing cells for both immunization and screening. One established clone - C19Mab-1 - proved to be useful in flow cytometry assays against lymphoma cell lines, such as BALL-1, P30/OHK, and Raji. Second, the extracellular domain of CD19 was immunized into mice, and enzyme-linked immunosorbent assays were performed for the first screening. One established clone - C19Mab-3 - was determined to be useful for Western blotting and immunohistochemical analysis. Due to their complementary utility, a combination of C19Mab-1 (established using CBIS) and C19Mab-3 (established using conventional method) could be useful for the pathological analysis of CD19.
AB - CD19 is a type I transmembrane glycoprotein belonging to the immunoglobulin superfamily. It is expressed in normal and neoplastic B cells, and it modulates the threshold of B cell activation for amplifying B cell receptor signaling. Blinatumomab (a CD3-CD19-bispecific T cell-engaging antibody) and tisagenlecleucel (genetically modified T cells that express a CD19 chimeric antigen receptor [CART-19]) provide significant benefits for patients with CD19-positive relapsed or refractory B cell malignancies. In this study, we first employed the Cell-Based Immunization and Screening (CBIS) method to produce anti-CD19 monoclonal antibodies using CD19-overexpressing cells for both immunization and screening. One established clone - C19Mab-1 - proved to be useful in flow cytometry assays against lymphoma cell lines, such as BALL-1, P30/OHK, and Raji. Second, the extracellular domain of CD19 was immunized into mice, and enzyme-linked immunosorbent assays were performed for the first screening. One established clone - C19Mab-3 - was determined to be useful for Western blotting and immunohistochemical analysis. Due to their complementary utility, a combination of C19Mab-1 (established using CBIS) and C19Mab-3 (established using conventional method) could be useful for the pathological analysis of CD19.
KW - CD19
KW - hybridoma production
KW - monoclonal antibody
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U2 - 10.1089/mab.2020.0003
DO - 10.1089/mab.2020.0003
M3 - Article
C2 - 32271687
AN - SCOPUS:85083278030
SN - 2167-9436
VL - 39
SP - 45
EP - 50
JO - Monoclonal Antibodies in Immunodiagnosis and Immunotherapy
JF - Monoclonal Antibodies in Immunodiagnosis and Immunotherapy
IS - 2
ER -